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Temozolomide CAS NO 85622-93-1
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CAS No.:85622-93-1
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Temozolomide CAS NO 85622-93-1 is an alkylating agent belonging to the imidazotetrazine class of compounds. It is a critical active pharmaceutical ingredient (API) valued for its ability to cross the blood-brain barrier and function as a prodrug, converting to its active metabolite under physiological conditions. This product is essential for pharmaceutical manufacturers and research institutions developing treatments for aggressive brain tumors, such as glioblastoma multiforme and astrocytoma, as well as for clinical research into other oncological applications.
Application
- Primary Pharmaceutical Ingredient: Manufacture of oral chemotherapy capsules for the treatment of newly diagnosed and refractory glioblastoma multiforme.
- Oncology Research & Development: Key intermediate in preclinical and clinical studies exploring novel cancer therapies and combination treatment regimens.
- Generic Drug Formulation: Sourcing for companies producing bioequivalent versions of established temozolomide-based medications.
- Clinical Trial Supply: Provision of high-purity API for Phase I-IV clinical trials investigating expanded indications.
- Reference Standard: Used as a certified reference material (CRM) in analytical laboratories for quality control and method validation.
- Investigational Formulations: Research into alternative delivery systems, such as injectable or implantable formulations for targeted therapy.
Basic Information
| Product Name | Temozolomide |
| CAS No. | 85622-93-1 |
| Molecular Formula | C6H6N6O2 |
| Molecular Weight | 194.15 g/mol |
| Synonyms | Temodal; Temodar; Methazolastone; 3,4-Dihydro-3-methyl-4-oxoimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide; CCRG 81045; M & B 39831; NSC 362856; TMZ |
| EINECS | Contact for details |
Quality Control
Our Temozolomide is manufactured under strict quality management systems. Each batch is tested to meet stringent specifications for identity, purity, and impurity profiles, aligning with major pharmacopeial standards (e.g., USP, EP). A comprehensive Certificate of Analysis (COA) is provided with each shipment, detailing results for assay, related substances, residual solvents, and other critical parameters to ensure reliability and consistency for your manufacturing and research needs.
Storage
Preserve in a tightly closed container, protected from light. Store at controlled room temperature, typically between 15°C and 25°C (59°F and 77°F), in a dry environment. The product is light-sensitive and should be handled under appropriate conditions to maintain stability.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to reference standard |
| Identification (HPLC) | Retention time matches reference |
| Assay (HPLC) | 98.0% - 102.0% (on anhydrous basis) |
| Related Substances (HPLC) | Individual impurity: NMT 0.5% Total impurities: NMT 2.0% |
| Water Content (KF) | NMT 1.0% |
| Residue on Ignition | NMT 0.1% |
| Heavy Metals | NMT 20 ppm |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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